C04 Arthro Muscotox NDC 63479-0304

NDC codes

FDA NDC Directory

Product NDC (as listed)63479-0304Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63479-0304Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
63479-0304-1	63479030401	30 mL in 1 BOTTLE, GLASS (63479-0304-1)Marketed from Dec 15, 1994

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): C04 Arthro MuscotoxSuffix: ARTHRO MUSCOTOX
Generic name (nonproprietary): actaea spicata, ammonium benzoicum, arnica montana, bellis perennis, berberis vulgaris, bryonia, chelidonium majus, chininum sulphuricum, dulcamara lignosa whole, echinacea purpurea, formica rufa, fraxinus excelsior leaf, lacticum acidum, ledum palustre, pulsatilla vulgaris, rhododendron chrysanthum, rhus toxicodendron, ruta graveolens, sarcolacticum acidum, symphytum officinale, uricum acidum
Active ingredients: Solanum dulcamara whole — 30 [hp_X]/mLEchinacea purpurea — 1 [hp_X]/mLRuta graveolens flowering top — 9 [hp_X]/mLActaea spicata root — 12 [hp_X]/mLFormica rufa — 30 [hp_X]/mLFraxinus excelsior leaf — 1 [hp_X]/mLLactic acid, Dl- — 30 [hp_X]/mLRhododendron aureum leaf — 12 [hp_X]/mLToxicodendron pubescens leaf — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLRhododendron tomentosum leafy twig — 6 [hp_X]/mLAmmonium benzoate — 9 [hp_X]/mLArnica montana — 30 [hp_X]/mLBerberis vulgaris root bark — 1 [hp_X]/mLBryonia alba root — 30 [hp_X]/mLLactic acid, L- — 15 [hp_X]/mLComfrey root — 9 [hp_X]/mLUric acid — 15 [hp_X]/mLBellis perennis — 12 [hp_X]/mLChelidonium majus — 1 [hp_X]/mLQuinine sulfate — 9 [hp_X]/mL
Dosage form: Solution/ drops
Route: Sublingual
Labeler: Apex Energetics Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 15, 1994
Listing expires: Dec 31, 2026
Identifiers: Product ID 63479-0304_0e76cd12-9f3e-c98f-e063-6394a90ad9fbSPL ID 0e76cd12-9f3e-c98f-e063-6394a90ad9fbSPL set ID bc907936-2151-19a8-e053-2a95a90ad97aUNII G72JA9DHK5, QI7G114Y98, N94C2U587S, 3FU86L9OS0, 55H0W83JO5, RC38362Q7M, 3B8D35Y7S4, IV92NQJ73U, 6IO182RP7A, I76KB35JEV, 877L01IZ0P, AC80WD7GPF, O80TY208ZW, 1TH8Q20J0U, T7J046YI2B, F9S9FFU82N, M9VVZ08EKQ, 268B43MJ25, 2HU33I03UY, 7E889U5RNN, KF7Z0E0Q2BUPC 0818960011703
Pharmacologic class: Antimalarial

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463479030401 followed by a unit qualifier and the quantity

Package 63479-0304-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Jan 8, 2024.

Indications (excerpt from the label)

Uses: For temporary relief of minor: joint pain* sore muscles* fatigue* stiff neck and joints* *Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)